Canonical Allele Identifier: PA645402211
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Met2491Val
CA048161
NM_001127510.3:c.7471A>G